A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2802852



Internal ID21248190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43696976..43696976hg38UCSC Ensembl
chr20:42325616..42325616hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13684281
Samples
Known GenesMYBL2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2802852
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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